Iodomethyl pivalate → HCID 88207701, compound
Reaction equation
[NH2:1][C:2]1[S:3][CH:4]=[C:5](/[C:7](=[N:34]/[OH:35])/[C:8]([NH:10][CH:11]2[C:32](=[O:33])[N:13]3[C:14]([C:29]([O-:31])=[O:30])=[C:15]([CH2:18][O:19][C:20]([N:22]4[CH2:26][CH2:25][CH2:24][C@H:23]4[CH2:27][OH:28])=[O:21])[CH2:16][S:17][C@H:12]23)=[O:9])[N:6]=1.[Na+].[C:37]([O:43][CH2:44]I)(=[O:42])[C:38]([CH3:41])([CH3:40])[CH3:39]>>[NH2:1][C:2]1[S:3][CH:4]=[C:5](/[C:7](=[N:34]/[OH:35])/[C:8]([NH:10][CH:11]2[C:32](=[O:33])[N:13]3[C:14]([C:29]([O:31][CH2:44][O:43][C:37](=[O:42])[C:38]([CH3:41])([CH3:40])[CH3:39])=[O:30])=[C:15]([CH2:18][O:19][C:20]([N:22]4[CH2:26][CH2:25][CH2:24][C@H:23]4[CH2:27][OH:28])=[O:21])[CH2:16][S:17][C@H:12]23)=[O:9])[N:6]=1Participants
3
Procedure
The compound obtained in Example 12 and iodomethyl pivalate were reacted, whereby the title compound was obtained.
Sources & evidence
- ORD record
- ord-fc7cfded9e8c49a6b76edb39deb3e363
- Source dataset
- uspto-grants-1996_10
- Patent number
- US05563265
Reaction notes
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